Category:Medical genetics task force articles
Pages in category "Medical genetics task force articles"
The following 200 pages are in this category, out of approximately 1,261 total. This list may not reflect recent changes.
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- Talk:Kabuki syndrome
- Talk:Emil Kakkis
- Talk:Kallmann syndrome
- Talk:Karyotype
- Talk:Katz syndrome
- Talk:KBG syndrome
- Talk:KCNQ2 developmental and epileptic encephalopathy
- Talk:Kearns–Sayre syndrome
- Talk:Har Gobind Khorana
- Talk:Kindler syndrome
- Talk:Kirner's deformity
- Talk:Uwe Klima
- Talk:Klinefelter syndrome
- Talk:Klippel–Feil syndrome
- Talk:Kniest dysplasia
- Talk:Kohlschütter–Tönz syndrome
- Talk:Koolen–De Vries syndrome
- Talk:Krabbe disease
- Talk:Kufor–Rakeb syndrome
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- Talk:Lachiewicz–Sibley syndrome
- Talk:Lactose intolerance
- Talk:Lafora disease
- Talk:Langer–Giedion syndrome
- Talk:Laron syndrome
- Talk:Larsen syndrome
- Talk:Late onset congenital adrenal hyperplasia
- Talk:Laurence–Moon syndrome
- Talk:Leber's hereditary optic neuropathy
- Talk:Leigh syndrome
- Talk:Michael J. Lenardo
- Talk:Lesch–Nyhan syndrome
- Talk:Lethal white syndrome
- Talk:Leukocyte adhesion deficiency
- Talk:Leukocyte adhesion deficiency-1
- Talk:Leukoencephalopathy with vanishing white matter
- Talk:Harvey Levy (academic)
- Talk:Leydig cell hypoplasia
- Talk:Li–Fraumeni syndrome
- Talk:Liddle's syndrome
- Talk:Lipid storage disorder
- Talk:Lipoid congenital adrenal hyperplasia
- Talk:List of congenital disorders
- Talk:List of disorders included in newborn screening programs
- Talk:List of genetic diseases
- Talk:List of genetic disorders
- Talk:List of OMIM disorder codes
- Talk:List of people diagnosed with coeliac disease
- Talk:List of people diagnosed with Crohn's disease
- Talk:List of people diagnosed with ulcerative colitis
- Talk:List of people with color blindness
- Category talk:List-Class medical genetics articles
- Talk:Loading control
- Talk:Loeys–Dietz syndrome
- Talk:Long QT syndrome
- Talk:Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency
- Talk:Long-term nonprogressor
- Talk:Low copy number
- Talk:Low copy repeats
- Category talk:Low-importance medical genetics articles
- Talk:Lowry-Wood syndrome
- Talk:Lubani Al Saleh Teebi syndrome
- Talk:Luscan-Lumish syndrome
- Talk:Lysinuric protein intolerance
M
- Talk:Madelung's deformity
- Talk:Mahvash disease
- Talk:Major histocompatibility complex, class II, DQ alpha 1
- Talk:Malignant hyperthermia
- Talk:Malonic aciduria
- Talk:Mandibulofacial dysostosis-microcephaly syndrome
- Talk:Mannosidosis
- Talk:Maple syrup urine disease
- Talk:Marfan syndrome
- Talk:Marinesco-Sjogren syndrome
- Talk:Marker chromosome
- Talk:Maternal influence on sex determination
- Talk:Michelle Maykin
- Talk:McCune–Albright syndrome
- Talk:McGillivray syndrome
- Talk:McKusick–Kaufman syndrome
- Talk:McLeod syndrome
- Talk:Meacham syndrome
- Talk:Mechanism of PCR
- Talk:Medical genetics
- Category talk:Medical genetics
- Category talk:Medical genetics articles by importance
- Category talk:Medical genetics articles by quality
- Talk:Medical genetics of Jews
- Category talk:Medical genetics task force
- Category talk:Medical genetics task force articles
- Category talk:Medical genetics task force participants
- Talk:Medium-chain acyl-coenzyme A dehydrogenase deficiency
- Talk:Meromelia
- Talk:MERRF syndrome
- Talk:Metachondromatosis
- Talk:Metachromatic leukodystrophy
- Talk:Methylmalonic acidemia with homocystinuria
- Talk:Methylmalonyl-CoA mutase deficiency
- Talk:Microcephalic primordial dwarfism, Montreal type
- Talk:Microcephaly
- Talk:Microcephaly deafness syndrome
- Talk:Microcephaly lymphoedema chorioretinal dysplasia
- Talk:Microchimerism
- Talk:Microcytic anemia
- Talk:Microdeletion syndrome
- Category talk:Mid-importance medical genetics articles
- Talk:Migraine
- Talk:Mild androgen insensitivity syndrome
- Talk:Miller–Dieker syndrome
- Talk:Minor physical anomalies
- Talk:Mir-390 microRNA precursor family
- Talk:Mir-590 microRNA precursor family
- Talk:Mir-618 microRNA precursor family
- Talk:Mir-624 microRNA precursor family
- Talk:Mir-625 microRNA precursor family
- Talk:Mir-633 microRNA precursor family
- Talk:Mir-636 microRNA precursor family
- Talk:Mir-638 microRNA precursor family
- Talk:Mir-650 microRNA precursor family
- Talk:Mir-652 microRNA precursor family
- Talk:Mir-663 microRNA precursor family
- Talk:Mir-708 microRNA precursor family
- Talk:Mir-711 microRNA precursor family
- Talk:Mir-3180 microRNA precursor family
- Talk:Mismatch repair cancer syndrome
- Talk:Missing heritability problem
- Talk:Mitochondrial biogenesis
- Talk:Mitochondrial complex II deficiency
- Talk:Mitochondrial disease
- Category talk:Mitochondrial diseases
- Talk:Mitochondrial myopathy–encephalopathy–lactic acidosis–stroke syndrome
- Talk:Mitochondrial trifunctional protein deficiency
- Talk:Moebius syndrome
- Category talk:Molecular biologists by nationality
- Talk:Molecular biology
- Talk:Molecular Biology
- Category talk:Molecular genetics
- Talk:Molecular risk assessment
- Talk:Molecular Xeroxing
- Talk:Molybdenum cofactor deficiency
- Talk:MOMO syndrome
- Talk:Mongolian idiocy
- Talk:Monogenic obesity
- Talk:Moonrise (Wolfson book)
- Talk:MORM syndrome
- Talk:D. Holmes Morton
- Talk:Mosaic loss of chromosome Y
- Talk:Roxana Moslehi
- Talk:Mouse models of Down syndrome
- Talk:MPI-CDG
- Talk:Mucolipidosis
- Talk:Mucopolysaccharidosis
- Talk:Mulibrey nanism
- Talk:Multifactorial disease
- Talk:Multifocal stenosing ulceration of the small intestine
- Talk:Multiple congenital anomalies-hypotonia-seizures syndrome
- Talk:Multiple endocrine neoplasia type 1
- Talk:Multiple endocrine neoplasia type 2
- Talk:Multiple sulfatase deficiency
- Talk:Muscular dystrophy
- Talk:Muscular dystrophy - Duchenne type
- Talk:Muscular Dystrophy Association
- Talk:Muscular dystrophy Duchenne type
- Category talk:Muscular dystrophy organizations
- Talk:Muscular dystrophy, duchenne
- Talk:Muscular dystrophy, Duchenne
- Talk:Mutational meltdown
- Talk:MUTYH-associated polyposis
- Talk:Myelokathexis
- Talk:Myeloperoxidase deficiency
- Talk:Myopathy
- Talk:Myopathy, X-linked, with excessive autophagy
- Talk:Myotonia congenita
- Talk:Myotonic dystrophy
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- Talk:N-Acetylglutamate synthase deficiency
- Category talk:NA-Class medical genetics articles
- Category talk:NA-importance medical genetics articles
- Talk:Nail–patella syndrome
- Talk:Emil Najman
- Talk:Nance–Horan syndrome
- Talk:National Bleeding Disorders Foundation
- Talk:National Society of Genetic Counselors
- Talk:NcRNA therapy
- Talk:Nemaline myopathy
- Talk:Neonatal adrenoleukodystrophy
- Talk:Neonatal hemochromatosis
- Talk:Neonatal teeth
- Talk:Neotenic complex syndrome
- Talk:Neurofibromatosis
- Talk:Neurofibromatosis type I
- Talk:Neurofibromatosis type II
- Talk:Neuropathy, ataxia, and retinitis pigmentosa
- Talk:Niemann–Pick disease
- Talk:Niemann–Pick disease type C
- Talk:Nijmegen breakage syndrome
- Talk:Noninvasive prenatal testing
- Talk:Nonsyndromic deafness
- Talk:Noonan syndrome
- Talk:Noonan syndrome with multiple lentigines
- Talk:Normal People Scare Me
- Talk:Norman–Roberts syndrome